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This research is an output from the Drugs for Neglected Diseases (DNDi) initiative
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Advice for manufacturers of Class I medical devices for placing products on the UK market
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
UK Health Security Agency's laboratories provide a comprehensive range of microbiological tests and services.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
This paper analyses implications for inflation, output and the exchange rate in the presence of domestic and external shocks
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